vardenafil

Generic: vardenafil

Labeler: zydus pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name vardenafil
Generic Name vardenafil
Labeler zydus pharmaceuticals usa inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

vardenafil hydrochloride trihydrate 5 mg/1

Manufacturer
Zydus Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 70710-1069
Product ID 70710-1069_a6417d62-c65a-49a5-a3c7-d9d178a36cb9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208960
Listing Expiration 2027-12-31
Marketing Start 2018-11-01

Pharmacologic Class

Classes
phosphodiesterase 5 inhibitor [epc] phosphodiesterase 5 inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 707101069
Hyphenated Format 70710-1069

Supplemental Identifiers

RxCUI
349478 349479 349480 402273
UPC
0370710106935
UNII
5M8S2CU0TS

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name vardenafil (source: ndc)
Generic Name vardenafil (source: ndc)
Application Number ANDA208960 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (70710-1069-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE (70710-1069-3)
  • 90 TABLET, FILM COATED in 1 BOTTLE (70710-1069-9)
source: ndc

Packages (3)

70710-1069-1 100 TABLET, FILM COATED in 1 BOTTLE (70710-1069-1) 70710-1069-3 30 TABLET, FILM COATED in 1 BOTTLE (70710-1069-3) 70710-1069-9 90 TABLET, FILM COATED in 1 BOTTLE (70710-1069-9)

Ingredients (1)

vardenafil hydrochloride trihydrate (5 mg/1)

Linked Drug Pages (1)

VARDENAFIL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a6417d62-c65a-49a5-a3c7-d9d178a36cb9", "openfda": {"upc": ["0370710106935"], "unii": ["5M8S2CU0TS"], "rxcui": ["349478", "349479", "349480", "402273"], "spl_set_id": ["5876e062-e604-42a7-99c3-5da30b8dac06"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70710-1069-1)", "package_ndc": "70710-1069-1", "marketing_start_date": "20181101"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (70710-1069-3)", "package_ndc": "70710-1069-3", "marketing_start_date": "20181101"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (70710-1069-9)", "package_ndc": "70710-1069-9", "marketing_start_date": "20181101"}], "brand_name": "VARDENAFIL", "product_id": "70710-1069_a6417d62-c65a-49a5-a3c7-d9d178a36cb9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "70710-1069", "generic_name": "VARDENAFIL", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VARDENAFIL", "active_ingredients": [{"name": "VARDENAFIL HYDROCHLORIDE TRIHYDRATE", "strength": "5 mg/1"}], "application_number": "ANDA208960", "marketing_category": "ANDA", "marketing_start_date": "20181101", "listing_expiration_date": "20271231"}